Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv5874902

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:401

Publication(s):Almarri et al. 2020

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 443 SVs from 32 studies. See in: genome view

Submitted genomic110,689,398-110,689,798

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5874902	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	110,689,398	110,689,798
nsv5874902	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	109,932,626	109,933,026

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17444385	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17444385	Submitted genomic		NC_000023.11:g.110 689398_110689798de l	GRCh38 (hg38)		NC_000023.11	ChrX	110,689,398	110,689,798
nssv17444385	Remapped	Perfect	NC_000023.10:g.109 932626_109933026de l	GRCh37.p13	First Pass	NC_000023.10	ChrX	109,932,626	109,933,026

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

You are here: NCBI